International audienceLaminopathies are a group of rare disorders due to mutation in LMNA gene. Depending on the mutation, they may affect striated muscles, adipose tissues, nerves or are multisystemic with various accelerated ageing syndromes. Although the diverse pathomechanisms responsible for laminopathies are not fully understood, several therapeutic approaches have been evaluated in patient cells or animal models, ranging from gene therapies to cell and drug therapies. This review is focused on these therapies with a strong focus on striated muscle laminopathies and premature ageing syndromes
International audienceLMNA-related Congenital Muscular Dystrophy (L-CMD) is the most severe form of ...
Laminopathies are a clinically heterogeneous group of disorders caused by mutations in LMNA. The mai...
Laminopathies are a clinically heterogeneous group of disorders caused by mutations in LMNA. The mai...
International audienceLaminopathies are a group of rare disorders due to mutation in LMNA gene. Depe...
LMNA-related disorders are caused by mutations in the LMNA gene, which encodes for the nuclear envel...
The lamin A/C (LMNA) gene codes for nuclear intermediate filaments constitutive of the nuclear lamin...
Lamins (LMNA) are the main proteins of the nuclear lamina considered to be the ancestors of all inte...
International audienceBackground:Variants in the LMNA gene, encoding lamins A/C, are responsible for...
Lamins (LMNA) are the main proteins of the nuclear lamina considered to be the ancestors of all inte...
Laminopathies are genetic diseases that encompass a wide spectrum of phenotypes with diverse tissue ...
Laminopathies belong to the group of diseases caused by mutations in genes encoding nuclear envelope...
Mutations in A-type lamins or lamin-binding proteins are involved in the pathogenesis of diseases re...
Laminopathies are a group of inherited disorders caused by mutations in the lamin A/C gene, and can ...
Laminopathies are a clinically heterogeneous group of disorders caused by mutations in LMNA. The mai...
Laminopathies are a clinically heterogeneous group of disorders caused by mutations in LMNA. The mai...
International audienceLMNA-related Congenital Muscular Dystrophy (L-CMD) is the most severe form of ...
Laminopathies are a clinically heterogeneous group of disorders caused by mutations in LMNA. The mai...
Laminopathies are a clinically heterogeneous group of disorders caused by mutations in LMNA. The mai...
International audienceLaminopathies are a group of rare disorders due to mutation in LMNA gene. Depe...
LMNA-related disorders are caused by mutations in the LMNA gene, which encodes for the nuclear envel...
The lamin A/C (LMNA) gene codes for nuclear intermediate filaments constitutive of the nuclear lamin...
Lamins (LMNA) are the main proteins of the nuclear lamina considered to be the ancestors of all inte...
International audienceBackground:Variants in the LMNA gene, encoding lamins A/C, are responsible for...
Lamins (LMNA) are the main proteins of the nuclear lamina considered to be the ancestors of all inte...
Laminopathies are genetic diseases that encompass a wide spectrum of phenotypes with diverse tissue ...
Laminopathies belong to the group of diseases caused by mutations in genes encoding nuclear envelope...
Mutations in A-type lamins or lamin-binding proteins are involved in the pathogenesis of diseases re...
Laminopathies are a group of inherited disorders caused by mutations in the lamin A/C gene, and can ...
Laminopathies are a clinically heterogeneous group of disorders caused by mutations in LMNA. The mai...
Laminopathies are a clinically heterogeneous group of disorders caused by mutations in LMNA. The mai...
International audienceLMNA-related Congenital Muscular Dystrophy (L-CMD) is the most severe form of ...
Laminopathies are a clinically heterogeneous group of disorders caused by mutations in LMNA. The mai...
Laminopathies are a clinically heterogeneous group of disorders caused by mutations in LMNA. The mai...